Dos Santos Domingues Alessandra, Selleski Nicole, Uenishi Rosa Harumi, Medeiros Ribeiro de Magalhães Cristina, Gandolfi Lenora, Pratesi Claudia B
Interdisciplinary Laboratory of Biosciences and Celiac Disease Research Center, School of Medicine, University of Brasilia, Brasilia, Brazil.
Post-graduate Program in Health Sciences, School of Health Sciences, University of Brasilia, Brasilia, Brazil.
BMJ Open. 2018 Feb 14;8(2):e018803. doi: 10.1136/bmjopen-2017-018803.
Kawasaki disease (KD) is a self-limited acute systemic vasculitis of unknown aetiology that predominantly affects infants and young children eventually associated with immunological abnormalities. Coeliac disease (CD) is an inflammatory autoimmune disease characterised by a permanent gluten intolerance, which affects genetically susceptible individuals of any age group, and can cause intestinal and systemic symptoms. Association of CD with KD has been previously described in a single study that disclosed a surprisingly high prevalence of CD in children with a history of KD.
To confirm the existence of a higher prevalence of CD among individuals with a history of KD, which would turn the screening for CD in patients with history of KD highly advisable.
Children with history of KD, diagnosed and followed at the Rheumatology Clinic of the Children's Hospital of Brasilia (Brasilia, Brazil).
This study included 110 children with history of KD and a control group composed of 110 presumably healthy children.
Participants underwent anti-transglutaminase and anti-endomysial antibodies tests and genetic typing for the presence of CD predisposing alleles (HLA-DQ2 and DQ8). Jejunal biopsy was performed when necessary, according the European Society of Paediatric Gastroenterology, Hepatology and Nutrition guidelines.
Diagnosis of CD was confirmed in one (0.91%) patient with KD by positive serological tests, presence of predisposing alleles and CD typical lesions on duodenal biopsy. All serological tests were negative among the controls. The prevalence of CD predisposing alleles among patients with KD was 29.09%, similar to the prevalence found among controls, 33.64%.
The detected CD prevalence (0.91%) does not confirm the existence of an association between KD and CD since this prevalence is similar to that found in the general population (≃1%).
川崎病(KD)是一种病因不明的自限性急性全身性血管炎,主要影响婴幼儿,最终与免疫异常相关。乳糜泻(CD)是一种炎症性自身免疫性疾病,其特征为对麸质永久不耐受,可影响任何年龄组的遗传易感个体,并可导致肠道和全身症状。此前在一项研究中曾描述过CD与KD的关联,该研究揭示KD病史患儿中CD的患病率出奇地高。
确认KD病史个体中CD患病率较高的情况是否存在,这将使得对KD病史患者进行CD筛查成为非常必要的措施。
在巴西利亚儿童医院(巴西利亚,巴西)风湿病诊所诊断并随访的有KD病史的儿童。
本研究纳入了110名有KD病史的儿童以及由110名推测健康的儿童组成的对照组。
参与者接受了抗转谷氨酰胺酶和抗肌内膜抗体检测以及CD易感等位基因(HLA-DQ2和DQ8)的基因分型。必要时根据欧洲儿科胃肠病学、肝病学和营养学会指南进行空肠活检。
一名KD患儿(0.91%)经血清学检测阳性、存在易感等位基因以及十二指肠活检出现CD典型病变而确诊为CD。对照组所有血清学检测均为阴性。KD患者中CD易感等位基因的患病率为29.09%,与对照组中发现的患病率33.64%相似。
检测到的CD患病率(0.91%)并未证实KD与CD之间存在关联,因为该患病率与普通人群中发现的患病率(约1%)相似。